Thomas Scholl
Impact in
- Genetics top 2%
- BRCA gene mutations in cancer
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
- Genetics 15
- BRCA gene mutations in cancer 10
- Genomic variations and chromosomal abnormalities 9
- Neurogenetic and Muscular Disorders Research 4
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- CRISPR and Genetic Engineering 7
- RNA and protein synthesis mechanisms 4
- Co-authors
- Brian E. Ward (11 shared papers)Amie M. Deffenbaugh (7 shared papers)Viatcheslav R. Akmaev (6 shared papers)Brant C. Hendrickson (11 shared papers)Julia Reid (3 shared papers)Jack L. Strominger (4 shared papers)Sanjeev K. Mahanta (4 shared papers)Dmitry Pruss (3 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (3 papers)Molecular Genetics and Metabolism (2 papers)Journal of Medical Genetics (2 papers)Cancer Research (2 papers)Journal of Molecular Diagnostics (2 papers)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Thomas Scholl
50 papers receiving 4.0k citations
Thomas Scholl's Hit Papers
Peers
Comparison fields: 5 of 124
- Genetics 675
- Pediatrics, Perinatology and Child Health 1.0k
- Genetics 1.5k
- Cancer Research 345
- Pathology and Forensic Medicine 332
Countries citing papers authored by Thomas Scholl
This map shows the geographic impact of Thomas Scholl's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Thomas Scholl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Scholl more than expected).
Fields of papers citing papers by Thomas Scholl
This network shows the impact of papers produced by Thomas Scholl. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Thomas Scholl. The network helps show where Thomas Scholl may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas Scholl, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis Hit paper breakdown → | 2012 | 1047 |
| 2 | Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens Hit paper breakdown → | 2011 | 541 |
| 3 | 2002 | 499 | |
| 4 | 2009 | 304 | |
| 5 | 2015 | 202 | |
| 6 | 2006 | 157 | |
| 7 | 2003 | 153 | |
| 8 | 2009 | 140 | |
| 9 | 1997 | 130 | |
| 10 | 1997 | 107 | |
| 11 | 2013 | 103 | |
| 12 | 2009 | 88 | |
| 13 | 2008 | 74 | |
| 14 | 2011 | 66 | |
| 15 | 2005 | 53 | |
| 16 | 2005 | 45 | |
| 17 | 2007 | 43 | |
| 18 | 1996 | 39 | |
| 19 | 2014 | 34 | |
| 20 | 1994 | 29 |
About Thomas Scholl
Thomas Scholl is a scholar working on Genetics, Molecular Biology, Genetics, Organic Chemistry and Immunology, having authored 50 papers that have together received 4.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Genomic variations and chromosomal abnormalities (9 papers), CRISPR and Genetic Engineering (7 papers), Immune Cell Function and Interaction (5 papers), T-cell and B-cell Immunology (5 papers), Genetic factors in colorectal cancer (4 papers), Neurogenetic and Muscular Disorders Research (4 papers) and RNA and protein synthesis mechanisms (4 papers). The work is most often cited by research in Genetics (675 citations), Pediatrics, Perinatology and Child Health (1.0k citations), Genetics (1.5k citations), Cancer Research (345 citations) and Pathology and Forensic Medicine (332 citations). Thomas Scholl has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Brian E. Ward, Amie M. Deffenbaugh, Viatcheslav R. Akmaev, Brant C. Hendrickson, Julia Reid, Jack L. Strominger, Sanjeev K. Mahanta, Dmitry Pruss, Elizabeth M. Rohlfs and Bernice A. Allitto. Their work appears in journals such as Proceedings of the National Academy of Sciences, Molecular Genetics and Metabolism, Journal of Medical Genetics, Cancer Research and Journal of Molecular Diagnostics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.